γ-γ符合测量系统的新型前端读出电路研制

研制了一种新型前端读出电路，用于重离子治癌装置中符合测量原型系统的研究和测试。电路主要包括能量链、时间链和数据处理单元。能量链由截止频率7 MHz的抗混叠滤波器和模数转换器(ADC)组成，形成波形采样电路；时间链由高速比较器构成的定时甄别电路和时间数字转换器（TDC）组成；数据处理单元基于现场可编程门阵列(FPGA)设计实现。电路的线性度优于0.8%，噪声小于0.8 mV（RMS）。配合LaBr3单晶体条测试，能量分辨为4.5%（FWHM），在与LYSO晶体阵列配合测试时，位置映射散点图清晰。该前端读出电路性能优于CAMAC系统，具有较好的实际应用前景。     

亲子乐园空调送风方式的数值模拟研究

大型综合室内亲子乐园属于高大空间,设有游乐设施和游戏的特殊性使得对空间的舒适性要求一致,但是送风气流遇阻严重,室内存在较多气流死角,影响室内空气质量和儿童健康。因此其空调设计不仅需要考虑温度、风速的空间均匀度,还要考虑各点的空气龄和PMV-PPD指标。以天津某亲子乐园为研究对象,利用scSTREAM软件对适用于该房间的辐射供冷加新风、置换通风、混合通风三种空调方式的送风效果进行数值模拟分析,从流场的均匀性、人员的热舒适性等方面对模拟结果进行探讨,研究结果表明辐射供冷加新风方式的空间均匀性和PMV指标最佳,混合通风方式的空气龄最小。     

5A06-O aluminium–magnesium alloy sheet warm hydroforming and optimization of process parameters

The uniaxial tensile test of the 5A06-O aluminium–magnesium (Al–Mg) alloy sheet was performed in the temperature range of 20–300 °C to obtain the true stress–true strain curves at different temperatures and strain rates. The constitutive model of 5A06-O Al–Mg alloy sheet with the temperature range from 150 to 300°C was established. Based on the test results, a unique finite element simulation platform for warm hydroforming of 5A06-O Al–Mg alloy was set up using the general finite element software MSC.Marc to simulate warm hydroforming of classic specimen, and a coupled thermo-mechanical finite element model for warm hydroforming of cylindrical cup was built up. Combined with the experiment, the influence of the temperature field distribution and loading conditions on the sheet formability was studied. The results show that the non-isothermal temperature distribution conditions can significantly improve the forming performance of the material. As the temperature increases, the impact of the punching speed on the forming becomes particularly obvious; the optimal values of the fluid pressure and blank holder force required for forming are reduced.     

A Complexing Agent to Enable a Wide-Temperature Range Bromine-Based Flow Battery for Stationary Energy Storage

Bromine-based flow batteries (Br-FBs) are considered one of the most promising energy storage systems due to their features of high energy density and low cost. However, they generally suffer from uncontrolled diffusion of corrosive bromine particularly at high temperatures. That is because the interaction between polybromide anions and the commonly used complexing agent (N–methyl–N–ethyl–pyrrolidinium bromide [MEP]) decreases with increasing temperatures, which causes serious self-discharge and capacity fade. Herein, a novel bromine complexing agent, 1–ethyl–2–methyl–pyridinium bromide (BCA), is introduced in Br-FBs to solve the above problems. It is proven that BCA can combine with polybromide anions very well even at a high temperature of 60 °C. Moreover, the BCA contributes to decreasing the electrochemical polarization of Br⁻/Br₂ couple, which in turn improves their power density. As a result, a zinc–bromine flow battery with BCA as the complexing agent can achieve a high energy efficiency of 84% at 40 mA cm⁻², even at high temperature of 60 °C and it can stably run for more than 400 cycles without obvious performance decay. This paper provides an effective complexing agent to enable a wide temperature range Br-FB.     

Comfort design and optimization of direct expansion multi-connected radiant air conditioning based on 3D flow field simulation

The air conditioning method based on radiation heat exchange has the characteristics of small vertical temperature gradient, high thermal comfort and energy saving, and has become a hot spot of attention. The Fluent numerical simulation, the experiment in this paper studies the direct expansion multi-line radiant air conditioner under the artificially simulated climate environment in winter heating, summer cooling and dehumidification. The temperature difference of the radiation + fresh air mode at the same time indoors under heating conditions is less than 2.5 °C, and the time to reach the indoor set temperature of 24 °C is about 2–3 h. Under cooling conditions, the temperature difference of the radiation + fresh air mode at the same time in the room is about 0.5–2 °C, and the time to reach the indoor set temperature of 26 °C is about 1–3 h. In the fresh air mode, the indoor temperature difference and response time at the same time are slightly larger than the radiation + fresh air mode. The freezing and dehumidification effect of fresh air is obvious, the moisture content of dehumidifying fresh air is between 6.3 and 10.5 g/kg, and the dehumidification efficiency can reach 50%. Under the same artificial simulated climate environment, the consumption of the three modes is not much different. When the outdoor temperature in heating conditions is higher than 9 °C, the fresh air mode can get better, and the radiation + fresh air mode can achieve better comfort when running indoors under various conditions.     

Near-Field Drives Long-Lived Shallow Trapping of Polymeric C3N4 for Efficient Photocatalytic Hydrogen Evolution

Undesired photoelectronic dormancy through active species decay is adverse to photoactivity enhancement. An insufficient extrinsic driving force leads to ultrafast deep charge trapping and photoactive species depopulation in carbon nitride (g-C₃N₄). Excitation of shallow trapping in g-C₃N₄ with long-lived excited states opens up the possibility of pursuing high-efficiency photocatalysis. Herein, a near-field-assisted model is constructed consisting of an In₂O₃-cube/g-C₃N₄ heterojunction associated with ultrafast photodynamic coupling. This In₂O₃-cube-induced near-field assistance system provides catalytic “hot areas”, efficiently enhances the lifetimes of excited states and shallow trapping in g-C₃N₄ and this favors an increased active species density. Optical simulations combined with time-resolved transient absorption spectroscopy shows there is a built-in charge transfer and the active species lifetimes are longer in the In₂O₃-cube/g-C₃N₄ hybrid. Besides these properties, the estimated overpotential and interfacial kinetics of the In₂O₃-cube/g-C₃N₄ hybrid co-promotes the liquid phase reaction and also helps in boosting the photocatalytic performance. The photocatalytic results exhibit a tremendous improvement (34-fold) for visible-light-driven hydrogen production. Near-field-assisted long-lived active species and the influences of trap states is a novel finding for enhancing (g-C₃N₄)-based photocatalytic performance.     

Real-time organic aerosol chemical speciation in the indoor environment using extractive electrospray ionization mass spectrometry

Understanding the sources and composition of organic aerosol (OA) in indoor environments requires rapid measurements, since many emissions and processes have short timescales. However, real-time molecular-level OA measurements have not been reported indoors. Here, we present quantitative measurements, at a time resolution of five seconds, of molecular ions corresponding to diverse aerosol-phase species, by applying extractive electrospray ionization mass spectrometry (EESI-MS) to indoor air analysis for the first time, as part of the highly instrumented HOMEChem field study. We demonstrate how the complex spectra of EESI-MS are screened in order to extract chemical information and investigate the possibility of interference from gas-phase semivolatile species. During experiments that simulated the Thanksgiving US holiday meal preparation, EESI-MS quantified multiple species, including fatty acids, carbohydrates, siloxanes, and phthalates. Intercomparisons with Aerosol Mass Spectrometer (AMS) and Scanning Mobility Particle Sizer suggest that EESI-MS quantified a large fraction of OA. Comparisons with FIGAERO-CIMS shows similar signal levels and good correlation, with a range of 100 for the relative sensitivities. Comparisons with SV-TAG for phthalates and with SV-TAG and AMS for total siloxanes also show strong correlation. EESI-MS observations can be used with gas-phase measurements to identify co-emitted gas- and aerosol-phase species, and this is demonstrated using complementary gas-phase PTR-MS observations.     

Droplet dynamics in a proton exchange membrane fuel cell flow field design with 3D geometry

Water management is crucial to achieve both high-performance and durability of proton exchange membrane fuel cell (PEMFC). Therefore, it is necessary to investigate the dynamic behavior of droplets in PEMFC channel for water management. In this paper, we explore the kinetics of droplets in a 3D flow field by experimental and theoretical analysis. More specifically, we examine the following four perspectives: 1) the movement and falling of droplets, and their force and deformation, 2) the superiority of 3D flow field drainage, 3) the pressure and viscous force under different scenarios including varying droplet sizes and velocities, and 4) the expression describing the shape change of droplets. The results show that the 3D flow field has a greater driving force on droplets and that their deformation affects the discharge of liquid water. Throughout the study, we provide better understanding of droplet dynamic in PEMFC gas channels. It enables to optimize the design and working conditions of these channels.     

Influence of electrostatic field on the interaction of AB5-type alloy LaNi4.4Al0.3Fe0.3 with hydrogen

The effect of the electrostatic field on hydrogen absorption is experimentally studied for the case of AB₅-type intermetallic compound LaNi_4.4Al_0.3Fe_0.3 with low equilibrium pressure. Experimental facility contained control and measurement system for PCT-isotherms and a non-conductive polymer vessel immersed in a bath of a thermostat with transformer oil. The test sample with 100 g of the activated alloy powder was used. Electrostatic field was created between a copper tube, which simultaneously served as a hydrogen inlet, connected to a high voltage source and a grounded nickel plate rolled in the form of a cylinder around the outer wall of the vessel. The electrodes were arranged coaxially, the maximum voltage on the internal electrode was 15 kV. The high voltage source also allowed changing the polarity on the internal electrode.It was found that the electrostatic field had no effect on the already established equilibrium in the hydrogen-alloy system at a voltage at the electrode up to 15 kV, regardless of the polarity. However, the process of hydrogen absorption is noticeably slowed down when a voltage of up to 15 kV with negative polarity is applied to the internal electrode, and the effect increases with increasing voltage. At a voltage of 15 kV and the positive polarity of the internal electrode, there was no noticeable effect on the hydrogen absorption process.